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1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Clear cell renal carcinoma
Ocular albinism with congenital sensorineural deafness

MITF MITF
TYR


COMMON
GENES
MITF



Citations in the biomedical literature:


Clear cell renal carcinoma
MITF
Ocular albinism with congenital sensorineural deafness
TYR



Clear cell renal carcinoma
Ocular albinism with congenital sensorineural deafness

Synonym(s):
- CCRCC
- Clear cell adenocarcinoma
- Clear cell renal cell adenocarcinoma
- Clear cell renal cell carcinoma

Synonym(s):
- Waardenburg syndrome type 2 with ocular albinism

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.